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BGC0000290NRPS

A-47934

Producing organism
Streptomyces toyocaensis
Taxonomy
BacteriaActinomycetotaActinomycetesKitasatosporalesStreptomycetaceaeStreptomyces
Biosynthetic class
NRPS (Type I)
Total steps
9
DOI
MIBiG entry
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A-47934
C58H44Cl3N7O21S1311.14 Da

Gene Cluster Map34 genes · 69,301 bp

AAAAAAAAmT10 kb69.3 kb visible · 69,301 bp total
Biosynthetic (core)
Biosynthetic (additional)
Regulatory
Transport
Resistance
Unknown
Domains
CCondensation (C)
AAdenylation (A)
PCPPeptidyl carrier (PCP)
CnCOM N-term
CcCOM C-term
TEThioesterase (TE)
EEpimerization (E)
ECHEnoyl-CoA hydratase
AmTAminotransferase I/II
XPutative domain (X)
TgrTIGR01720

Pathway Graphsteps arranged in biosynthetic order

9 steps · 8 edges
Step 1M1
AAM80539.1
Step 2M2
AAM80539.1
+hydroxyphenylglyc…
Step 3M3
AAM80538.1
+Tyrosine
Step 4M4
AAM80537.1
+3,5-dihydroxyphen…
Step 5M5
AAM80537.1
+hydroxyphenylglyc…
Step 6M6
AAM80537.1
+hydroxyphenylglyc…
Step 7M7
AAM80536.1
+Tyrosine
Step 8TE
AAM80536.1,AAM80531.1,A…
Step 9
?
Starting stepIntermediateFinal productModuleLoadingTENo modulePKS stepNRPS stepTailoring/otherScroll to pan · Wheel to zoom

Biosynthetic Reactions9 steps

StepProduct IDEnzymeModuleSubstrateProduct SMILESNotes
1290-1AAM80539.1M1
OC([C@@H](C1=CC=C(O)C=C1)N)=O
2290-2AAM80539.1M2
290-1;hydroxyphenylglycine
from: 290-1
OC(C(CC1=CC(Cl)=C(O)C=C1)NC([C@@H](C2=CC=C(O)C=C2)N)=O)=O
3290-3AAM80538.1M3
290-2;Tyrosine
from: 290-2
OC(C(C1=CC(O)=CC(O)=C1)NC(C(CC2=CC(Cl)=C(O)C=C2)NC([C@@H](C3=CC=C(O)C=C3)N)=O)=O)=O
4290-4AAM80537.1M4
290-3;3,5-dihydroxyphenylglycine
from: 290-3
OC(C(C1=CC=C(O)C=C1)NC(C(C2=CC(O)=CC(O)=C2)NC(C(CC3=CC(Cl)=C(O)C=C3)NC([C@@H](C4=CC=C(O)C=C4)N)=O)=O)=O)=O
5290-5AAM80537.1M5
290-4;hydroxyphenylglycine
from: 290-4
OC([C@@H](C1=CC(Cl)=C(O)C=C1)NC(C(C2=CC=C(O)C=C2)NC(C(C3=CC(O)=CC(O)=C3)NC(C(CC4=CC(Cl)=C(O)C=C4)NC([C@@H](C5=CC=C(O)C=C5)N)=O)=O)=O)=O)=O
6290-6AAM80537.1M6
290-5;hydroxyphenylglycine
from: 290-5
OC([C@H]([C@@H](C1=CC=C(O)C(Cl)=C1)O)NC([C@@H](C2=CC(Cl)=C(O)C=C2)NC(C(C3=CC=C(O)C=C3)NC(C(C4=CC(O)=CC(O)=C4)NC(C(CC5=CC(Cl)=C(O)C=C5)NC([C@@H](C6=CC=C(O)C=C6)N)=O)=O)=O)=O)=O)=O
7290-7AAM80536.1M7
290-6;Tyrosine
from: 290-6
O=C(O)C(NC([C@H]([C@@H](C1=CC=C(O)C(Cl)=C1)O)NC([C@@H](C2=CC(Cl)=C(O)C=C2)NC(C(C3=CC=C(O)C=C3)NC(C(C4=CC(O)=CC(O)=C4)NC(C(CC5=CC(Cl)=C(O)C=C5)NC([C@@H](C6=CC=C(O)C=C6)N)=O)=O)=O)=O)=O)=O)C7=CC(O)=CC(O)=C7
8290-8AAM80536.1,AAM80531.1,AAM80534.1,AAM80533.1,AAM80535.1TE
290-7
from: 290-7
OC1=CC=C([C@@H](N)C2=O)C=C1OC3=CC(C(C(N[C@H]4C(N[C@H](C5=CC6=C(O)C(Cl)=C5)C(NC([C@H](O)C7=CC=C(O8)C(Cl)=C7)C(N[C@H](C(O)=O)C9=CC(O)=CC(O)=C96)=O)=O)=O)=O)NC([C@H](N2)CC%10=CC=C(OC%11=C(O)C8=CC4=C%11)C=C%10Cl)=O)=CC(O)=C3
9290?
290-8
from: 290-8
N[C@@H](C1=O)C2=CC=C(OS(O)(=O)=O)C(OC3=CC(C(C(N[C@H]4C(N[C@H](C5=CC6=C(O)C(Cl)=C5)C(NC([C@H](O)C7=CC=C(O8)C(Cl)=C7)C(N[C@H](C(O)=O)C9=CC(O)=CC(O)=C96)=O)=O)=O)=O)NC([C@H](N1)CC%10=CC=C(OC%11=C(O)C8=CC4=C%11)C=C%10Cl)=O)=CC(O)=C3)=C2
Click any row to view the chemical structure · Click a module badge (M1, TE…) to view domain architecture